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Variant : CV157309 (GRCh38/hg38 7q34(chr7:142355688-142553299)x1) Homo sapiens

Symbol: CV157309
Name: GRCh38/hg38 7q34(chr7:142355688-142553299)x1
Condition: See cases [RCV000136726]
Clinical Significance: benign
Last Evaluated: 10/01/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR11400   TRB   TRBV10-1   TRBV10-2   TRBV10-3   TRBV11-1   TRBV11-2   TRBV13   TRBV5-4   TRBV5-5   TRBV5-6   TRBV5-7   TRBV6-4   TRBV6-5   TRBV6-6   TRBV6-8   TRBV7-3   TRBV7-4   TRBV7-6   TRBV7-7   TRBV7-9   TRBV9  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_142355688)_(142553299_?)del
Human AssemblyChrPosition (strand)Source
GRCh387142,355,688 - 142,553,299CLINVAR
Build 367141,723,794 - 141,941,891CLINVAR
Cytogenetic Map77q34CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9484287
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.